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rs13098911

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs13098911(C;T)
Make rs13098911(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position46193709
is asnp
is mentioned by
dbSNPrs13098911
ebirs13098911
HLIrs13098911
Exacrs13098911
Varsomers13098911
Maprs13098911
PheGenIrs13098911
hapmaprs13098911
1000 genomesrs13098911
hgdprs13098911
ensemblrs13098911
gopubmedrs13098911
geneviewrs13098911
scholarrs13098911
googlers13098911
pharmgkbrs13098911
gwascentralrs13098911
openSNPrs13098911
23andMers13098911
23andMe allrs13098911
SNP Nexus

SNPshotrs13098911
SNPdbers13098911
MSV3drs13098911
GWAS Ctlgrs13098911
GMAF0.06015
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20190752OA-icon.png]
Trait Celiac disease
Title Multiple common variants for celiac disease influencing immune gene expression
Risk Allele A
P-val 3E-17
Odds Ratio 1.30 [1.23-1.39]